gudid Primary ID: 300-103

5P NAVY HI PULL HEADCAP *O (UDI 300-103)

Manufactured by Great Lakes Dental Technologies, Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The 5P NAVY HI PULL HEADCAP *O (Model/Catalog Number: 300-103) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification DZB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 300-103
Product Code / EMDN: DZB
Device Name: 5P NAVY HI PULL HEADCAP *O
Database Sync Date: 2026-08-09 09:14:54

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of 5P NAVY HI PULL HEADCAP *O?

The registered manufacturer of record for 5P NAVY HI PULL HEADCAP *O is Great Lakes Dental Technologies, Ltd..

What is the Primary UDI-DI identifier for 5P NAVY HI PULL HEADCAP *O?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 300-103.

What classification code is assigned to this device?

This device is registered under product classification code DZB.

Similar Classification Devices (DZB)

Other Devices by Great Lakes Dental Technologies, Ltd.

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